R. Maranta

Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

A. Anarat, G. Ardissino, G. Ghiggeri, 2013, Kidney international.

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.

G. Remuzzi, P. Zipfel, I. M. van der Meer, 2010, Clinical journal of the American Society of Nephrology : CJASN.

Localization of Mesenchymal Stromal Cells Dictates Their Immune or Proinflammatory Effects in Kidney Transplantation

N. Perico, G. Remuzzi, C. Rota, 2012, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

MYO1E mutations and childhood familial focal segmental glomerulosclerosis.

G. Remuzzi, F. Macciardi, A. Benigni, 2011, The New England journal of medicine.

Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation

A. Torroni, A. Achilli, M. Pala, 2009, BMC Evolutionary Biology.

Discordant phenotype in monozygotic twins with renal coloboma syndrome and a PAX2 mutation

G. Remuzzi, E. Daina, P. Iatropoulos, 2012, Pediatric Nephrology.

Molecular Basis of Factor H R1210C Association with Ocular and Renal Diseases.

S. Rodríguez de Córdoba, M. Noris, M. Blasco, 2016, Journal of the American Society of Nephrology : JASN.